US4857322A - Wood preservative - Google Patents

Wood preservative Download PDF

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Publication number
US4857322A
US4857322A US07/118,011 US11801187A US4857322A US 4857322 A US4857322 A US 4857322A US 11801187 A US11801187 A US 11801187A US 4857322 A US4857322 A US 4857322A
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Prior art keywords
copper
preservative
acid
wood
water
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US07/118,011
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Reimer Goettsche
Hans-Norbert Marx
Wendelin Hettler
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Dr Wolman GmbH
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Dr Wolman GmbH
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Assigned to DR. WOLMAN GMBH reassignment DR. WOLMAN GMBH ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: GOETTSCHE, REIMER, HETTLER, WENDELIN, MARX, HANS-NORBERT
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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/16—Heavy metals; Compounds thereof
    • A01N59/20—Copper
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/14—Boron; Compounds thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
    • B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
    • B27K3/16—Inorganic impregnating agents
    • B27K3/22—Compounds of zinc or copper
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
    • B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
    • B27K3/34—Organic impregnating agents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
    • B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
    • B27K3/52—Impregnating agents containing mixtures of inorganic and organic compounds

Definitions

  • the present invention relates to a wood preservative, for example in the form of an aqueous solution, which contains a copper compound, an aliphatic carboxylic acid and a polyamine.
  • Wood preservatives based on alkanolamines, copper compounds and aliphatic C 6 -C 18 -monocarboxylic acids are known (Australian Pat. No. 519,146).
  • aqueous solutions of this wood preservative When wood is impregnated by large-scale industrial processes, for example the pressure impregnation process, with aqueous solutions of this wood preservative, the depth of penetration and the distribution of the copper carboxylates which form in the wood are not sufficient to ensure preservation of the wood, for example in the case of round woods, such as poles or palisades, in particular when they are used in permanent contact with the ground.
  • a depth of penetration of copper of only about 10 mm has been achieved.
  • aliphatic polyamines examples include aliphatic polyamines, alkylenepolyamines of 3 to 9 carbon atoms and 2 to 4 nitrogen atoms, 1,3-diaminopropane, 1-methylamino-3-aminopropane, dipropylenetriamine (3,3'-diaminodipropylamine) and tripropylenetetramine. 1,3-diaminopropane is preferred.
  • Suitable aliphatic carboxylic acids are C 5 -C 20 -monocarboxylic acids, such as hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, 2-ethylpentanoic acid, 2-ethylhexanoic acid, 2-ethylheptanoic acid, isooctanoic acid, isononanoic acid, isodecanoic acid and Versatic acids (highly branched monocarboxylic acids), and C 5 -C 20 -dicarboxylic acids, eg. decanedicarboxylic acid.
  • Polycarboxylic acids such as polyacrylic acids, are also suitable. 2-ethylhexanoic acid is preferred.
  • Suitable copper compounds are water-soluble or insoluble compounds (eg. copper salts, such as copper sulfate, copper hydroxide, copper carbonate, copper acetate, copper borate, copper fluoride and copper fluoborate). Copper carbonate is preferred.
  • copper salts such as copper sulfate, copper hydroxide, copper carbonate, copper acetate, copper borate, copper fluoride and copper fluoborate. Copper carbonate is preferred.
  • Some of the copper can, for example, also be replaced by an appropriate zinc compound.
  • the water-dilutable agents contain the copper, calculated as the element, in an amount of from 1 to 15% by weight.
  • An example of a quaternary ammonium compound is a compound of the general formula (R 1 R 2 R 3 R 4 N) + Z--, where R 1 is alkyl of 8 to 20, in particular 12 to 20, carbon atoms, or benzyl which is unsubstituted or substituted by C 1 -C 20 -alkyl or halogen, R 2 is C 1 -C 6 -alkyl or C 3 -C 19 -alkoxyalkyl, R 3 is C 1 -C 6 -alkyl or C 1 -C 4 -alkoxy and R 4 is C 1 -C 20 -alkyl, or two radicals R 1 to R 4 , together with the nitrogen atom, form a heterocyclic radical which contains four or five atoms, one or two nitrogen atoms and one, two or three double bonds, the carbon atoms being unsubstituted or substituted by C 1 -C 4 -alkyl or halogen, and Z is an acid radical.
  • Suitable concentrates contain, for example,
  • the concentrates which may be in the form of pastes or viscous solutions (if appropriate, also in the form of a solid salt), are most readily prepared by initially taking a polyamine, with or without water, and dissolving the carboxylic acids and, where relevant, the salts containing fungicidal anions and/or salts of N-cyclohexyldihydroxydiazenium oxide therein. The copper compounds then dissolve in this mixture with complex formation.
  • pine palisades having a length of 1.20 m, a diameter of 15-20 cm and a sapwood width of more than 30 mm were impregnated by the pressure impregnation method (1 hour under reduced pressure, 2 hours under superatmospheric pressure).
  • the impregnated woods were cut open in the middle, the cut surface was treated with diethyl dithiocarbamate/Na salt solution (brown coloration with copper) and the depth of penetration of the copper was measured. 2 palisades were impregnated per test.
  • the water absorption of the impregnated blocks as a result of further impregnation with water was determined by weight and compared with that of blocks which had been treated exclusively with water and correspondingly dried.
  • the further water absorption of these blocks was set at 100 for purposes of comparison. The measurements were carried out using 10 blocks in each case. It was found that the impregnated blocks absorbed less water than the blocks treated with water.

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Inorganic Chemistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Chemical And Physical Treatments For Wood And The Like (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Wood preservatives based on a copper compound and an aliphatic carboxylic acid and additionally containing a polyamine, and a method for preserving wood with these preservatives.

Description

The present invention relates to a wood preservative, for example in the form of an aqueous solution, which contains a copper compound, an aliphatic carboxylic acid and a polyamine.
Wood preservatives based on alkanolamines, copper compounds and aliphatic C6 -C18 -monocarboxylic acids are known (Australian Pat. No. 519,146). When wood is impregnated by large-scale industrial processes, for example the pressure impregnation process, with aqueous solutions of this wood preservative, the depth of penetration and the distribution of the copper carboxylates which form in the wood are not sufficient to ensure preservation of the wood, for example in the case of round woods, such as poles or palisades, in particular when they are used in permanent contact with the ground. For example, a depth of penetration of copper of only about 10 mm has been achieved.
We have found that the abovementioned disadvantages do not occur in wood preservatives based on copper compounds, aliphatic carboxylic acids and polyamines. Examples of particularly suitable polyamines in this case are aliphatic polyamines, alkylenepolyamines of 3 to 9 carbon atoms and 2 to 4 nitrogen atoms, 1,3-diaminopropane, 1-methylamino-3-aminopropane, dipropylenetriamine (3,3'-diaminodipropylamine) and tripropylenetetramine. 1,3-diaminopropane is preferred.
Examples of suitable aliphatic carboxylic acids are C5 -C20 -monocarboxylic acids, such as hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, 2-ethylpentanoic acid, 2-ethylhexanoic acid, 2-ethylheptanoic acid, isooctanoic acid, isononanoic acid, isodecanoic acid and Versatic acids (highly branched monocarboxylic acids), and C5 -C20 -dicarboxylic acids, eg. decanedicarboxylic acid. Polycarboxylic acids, such as polyacrylic acids, are also suitable. 2-ethylhexanoic acid is preferred.
These acids react with copper to form water-insoluble salts, which are dissolved in the alkaline medium as a result of the complex-forming action of the abovementioned amines.
Suitable copper compounds are water-soluble or insoluble compounds (eg. copper salts, such as copper sulfate, copper hydroxide, copper carbonate, copper acetate, copper borate, copper fluoride and copper fluoborate). Copper carbonate is preferred.
Some of the copper can, for example, also be replaced by an appropriate zinc compound.
In concentrated form, the water-dilutable agents contain the copper, calculated as the element, in an amount of from 1 to 15% by weight.
Additional anions capable of diffusion, eg. borates, fluorides or borofluorides, may be present; after impregnation of the wood, these anions diffuse and thus protect regions inaccessible to an impregnation, such as the heartwood.
The action of the wood preservative can be supplemented, for example, by salts of N-cyclohexyldihydroxydiazenium oxide, for example the copper salt or the potassium salt. Combination with quaternary ammonium compounds is also suitable for this purpose.
An example of a quaternary ammonium compound is a compound of the general formula (R1 R2 R3 R4 N)+ Z--, where R1 is alkyl of 8 to 20, in particular 12 to 20, carbon atoms, or benzyl which is unsubstituted or substituted by C1 -C20 -alkyl or halogen, R2 is C1 -C6 -alkyl or C3 -C19 -alkoxyalkyl, R3 is C1 -C6 -alkyl or C1 -C4 -alkoxy and R4 is C1 -C20 -alkyl, or two radicals R1 to R4, together with the nitrogen atom, form a heterocyclic radical which contains four or five atoms, one or two nitrogen atoms and one, two or three double bonds, the carbon atoms being unsubstituted or substituted by C1 -C4 -alkyl or halogen, and Z is an acid radical.
Suitable concentrates contain, for example,
5-40% of a copper compound,
10-40% of a carboxylic acid/polycarboxylic acid,
5-40% of a polyamine,
up to 40% of a fungicidal anion capable of diffusion,
up to 75% of a quaternary ammonium salt and
up to 30% of a salt of N-cyclohexyldihydroxydiazenium oxide,
the sum being 100 (% by weight) in each case.
If necessary, minor amounts of other components, such as other amines, ammonia, wetting agents, water softeners (nitriloacetic acid, etc.) and, if required, water may be present, the amounts of the latter however being kept small where possible and essentially serving to facilitate handling.
However, the invention also relates to the impregnation solutions obtainable by dilution of the concentrates with water, in accordance with the required concentrations for use and depending on the impregnation method and the degree of danger to the wood.
The concentrates, which may be in the form of pastes or viscous solutions (if appropriate, also in the form of a solid salt), are most readily prepared by initially taking a polyamine, with or without water, and dissolving the carboxylic acids and, where relevant, the salts containing fungicidal anions and/or salts of N-cyclohexyldihydroxydiazenium oxide therein. The copper compounds then dissolve in this mixture with complex formation. The alkalinity of the concentrates is adjusted, on the one hand, to ensure that sufficient polyamine is present to dissolve the copper compound and, on the other hand, by adding, for example, further polyamines, amines or alkali metal hydroxides to bring the pH of the dilute solutions for use to, in general, above 8, in particular from 8.5 to 10 (concentration-dependent). When impregnation is carried out, the copper compound penetrates thoroughly into the wood, the major part of the copper (about 70-95%) being fixed in the wood.
During impregnation, the wood preservatives penetrate the wood thoroughly, and the impregnatable regions of the wood (for example sapwood in pine) are entirely impregnated in the pressure impregnation process. Furthermore, penetration of water into the impregnated wood is more difficult, and the impregnated wood thus becomes more highly water-repellent.
To determine the depth of penetration, pine palisades having a length of 1.20 m, a diameter of 15-20 cm and a sapwood width of more than 30 mm were impregnated by the pressure impregnation method (1 hour under reduced pressure, 2 hours under superatmospheric pressure). To determine the depth of penetration of copper, the impregnated woods were cut open in the middle, the cut surface was treated with diethyl dithiocarbamate/Na salt solution (brown coloration with copper) and the depth of penetration of the copper was measured. 2 palisades were impregnated per test.
KNOWN COMPARATIVE EXAMPLES 
______________________________________                                    
Wood preservative I                                                       
               13.3%   Copper carbonate                                   
               30.0%   Ethanolamine                                       
               5.0%    Boric acid                                         
               36.7%   2-ethylhexanoic acid                               
               15.0%   Water                                              
               100%                                                       
Concentration for use:                                                    
               4%                                                         
The following mean penetration depths were determined:                    
13.7 mm and 12.0 mm                                                       
Wood preservative II                                                      
               13.3%   Copper carbonate                                   
               30.0%   Ethanolamine                                       
               36.7%   Polyacrylic acid (n =                              
                       10-100)                                            
               20.0%   Water                                              
               100%                                                       
Concentration for use:                                                    
               4%                                                         
Mean penetration depths: 9.1 mm and 14.0 mm                               
Examples according to the invention                                       
Example 1      13.3%   Copper carbonate                                   
               28.0%   Dipropylenetriamine                                
               10.0%   Boric acid                                         
               42.0%   Nonanoic acid                                      
               6.7%    Water                                              
               100%                                                       
Concentration for use:                                                    
               4%                                                         
Mean penetration depths: 32.1 mm and 29.3 mm                              
Example 2      13.3%   Copper carbonate                                   
               28.0%   Dipropylenetriamine                                
               10.0%   Boric acid                                         
               36.7%   Isooctanoic acid                                   
               12.0%   Water                                              
               100%                                                       
Concentration for use:                                                    
               4%                                                         
Mean penetration depths: 41.0 mm and 34.1 mm                              
Example 3      10.0%   Copper carbonate                                   
               16.5%   1,3-diaminopropane                                 
               27.5%   2-ethylhexanoic acid                               
               4.0%    Boric acid                                         
               2.5%    Nitrilotriacetic acid                              
               5.0%    Potassium salt of N--                              
                       cyclohexyldihydroxy-                               
                       diazenium oxide                                    
                34.5%  Water                                              
               100%                                                       
Concentration for use:                                                    
               4%                                                         
Mean penetration depths: 29.1 mm and 37.2 mm                              
Example 4      13.3%   Copper carbonate                                   
               13.3%   1,3-diaminopropane                                 
               11.4%   1-methylamino-3-amino-                             
                       propane                                            
               10.0%   Boric acid                                         
               36.7%   2-ethylhexanoic acid                               
               15.3%   Water                                              
               100%                                                       
Concentration for use:                                                    
               4%                                                         
Mean penetration depths: 36.5 mm and 28.3 mm                              
Example 5      10.0%   Copper carbonate                                   
               15.0%   Tripropylenetetramine                              
               10.0%   Dipropylenetriamine                                
               25.0%   2-ethylhexanoic acid                               
               20.0%   Dimethyl--C.sub.12 --                              
                       alkylbenzyl-                                       
                       ammonium chloride                                  
               20.0%   Water                                              
               100%                                                       
Concentration for use:                                                    
               4%                                                         
______________________________________
The following mean penetration depths were determined: 35.2 mm and 40.1 mm
Furthermore, pine sapwood blocks were impregnated with novel solutions and stored for about 6 weeks for fixing and drying (water content 16-18%).
The water absorption of the impregnated blocks as a result of further impregnation with water was determined by weight and compared with that of blocks which had been treated exclusively with water and correspondingly dried. The further water absorption of these blocks (blank test) was set at 100 for purposes of comparison. The measurements were carried out using 10 blocks in each case. It was found that the impregnated blocks absorbed less water than the blocks treated with water.

Claims (14)

We claim:
1. A wood preservative, comprising:
(a) about 5-40 wt.% of a copper compound,
(b) about 10-40 wt.% of an aliphatic monocarboxylic acid, aliphatic dicarboxylic acid or polycarboxylic acid, or a mixture thereof, and
(c) about 5-40 wt.% of a polyamine containing 3-9 carbon atoms, 2-4 nitrogen atoms and containing at least one primary amino group, based upon the total weight of the mixture.
2. The preservative as claimed in claim 1, wherein the monocarboxylic acid is 2-ethylhexanoic acid.
3. The preservative as claimed in claim 1, wherein the monocarboxylic acid is an isooctanoic acid.
4. The preservative as claimed in claim 1, wherein the copper compound is copper oxide, copper hydroxide or copper carbonate.
5. The preservative as claimed in claim 1, wherein the polyamine is 1,3-diaminopropane.
6. The preservative as claimed in claim 1, which additionally contains an alkali metal salt or a copper salt of N-cyclohexyldihydroxydiazenium oxide.
7. A method of protecting wood, which comprises treating the wood with an impregnation solution comprising an aqueous solution containing an effective amount of the wood preservative of claim 1.
8. The preservative as claimed in claim 1, wherein said monocarboxylic acid is a C5 -C20 -monocarboxylic acid.
9. The preservative as claimed in claim 1, wherein said dicarboxylic acid is a C5 -C20 -dicarboxylic acid.
10. The preservative as claimed in claim 1, wherein said polycarboxylic acid is polyacrylic acid.
11. The preservative as claimed in claim 1, wherein said copper compound is selected from the group consisting of copper sulfate, copper hydroxide, copper carbonate, copper acetate, copper borate, copper fluoride and copper fluoborate.
12. The preservative as claimed in claim 1, which has a pH of at least 8.0.
13. The preservative as claimed in claim 12, which has a pH in the range of 8.5 to 10.
14. The method as claimed in claim 7, wherein said treatment comprises subjecting said wood to said wood preservative using the pressure impregnation method.
US07/118,011 1986-11-14 1987-11-09 Wood preservative Expired - Lifetime US4857322A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19863639063 DE3639063A1 (en) 1986-11-14 1986-11-14 WOOD PRESERVATIVES
DE3639063 1986-11-14

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US4857322A true US4857322A (en) 1989-08-15

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US (1) US4857322A (en)
EP (1) EP0270848B1 (en)
AT (1) ATE64889T1 (en)
AU (1) AU599165B2 (en)
CA (1) CA1305834C (en)
DE (2) DE3639063A1 (en)
ES (1) ES2022863B3 (en)
GR (1) GR3002257T3 (en)
NZ (1) NZ222526A (en)

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US5426121A (en) * 1994-10-04 1995-06-20 Akzo Nobel N.V. Wood preservation formulation comprising complex of a copper cation and alkoxylated diamine
US5444093A (en) * 1989-11-11 1995-08-22 Dr. Wolman Gmbh Wood preservatives
US5460751A (en) * 1993-09-02 1995-10-24 Union Carbide Chemicals & Plastics Technology Corporation Compositions for the preservation of timber products
US5916356A (en) * 1991-08-01 1999-06-29 Hickson International Plc Preservatives for wood and other cellulosic materials
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US6294071B1 (en) 2000-01-07 2001-09-25 Huntsman Petrochemical Corporation Methods of forming copper solutions
US6340384B1 (en) 1999-05-24 2002-01-22 Lonza Inc. Copper/amine oxide wood preservatives
US6352583B1 (en) * 1997-03-05 2002-03-05 Dr. Wolman Gmbh Wood preservative for subsequent application
US6375727B1 (en) 1999-05-24 2002-04-23 Lonza Inc. Amine oxide/iodine containing blends for wood preservation
US6448279B1 (en) 1999-05-24 2002-09-10 Lonza Inc. Isothiazolone/amine oxide wood preservatives
US6508869B2 (en) 2000-06-30 2003-01-21 Lonza Inc. Boron compound/amine oxide compositions
US6527981B1 (en) 1999-05-24 2003-03-04 Lonza Inc. Azole/amine oxide preservatives
US6572788B2 (en) 2000-05-24 2003-06-03 Lonza, Inc. Amine oxide wood preservatives
US20040016909A1 (en) * 2002-07-26 2004-01-29 Jun Zhang Polymeric wood preservative compositions
US20050000387A1 (en) * 2003-07-02 2005-01-06 Ying Wang Wood preservative with alkaline copper quaternary
WO2006031207A1 (en) * 2004-09-17 2006-03-23 Stojan Kosmerl Solution for wood preservation
US7160606B2 (en) 2001-09-17 2007-01-09 Genics Inc. Method of treating building materials with boron and building materials
US20070021385A1 (en) * 2005-07-21 2007-01-25 Jun Zhang Compositions and methods for wood preservation
US20070135391A1 (en) * 2003-11-11 2007-06-14 Basf Aktiengesellschaft Microbicidal compositions and their use
US20080131666A1 (en) * 2003-07-31 2008-06-05 Fox Roger F Penetration improvement of copper amine solutions into dried wood by addition of carbon dioxide
US20080175913A1 (en) * 2007-01-09 2008-07-24 Jun Zhang Wood preservative compositions comprising isothiazolone-pyrethroids
US20080210121A1 (en) * 2003-04-09 2008-09-04 Jun Zhang Micronized wood preservative formulations
US20090162410A1 (en) * 2007-12-21 2009-06-25 Jun Zhang Process for preparing fine particle dispersion for wood preservation
US20090211487A1 (en) * 2005-06-29 2009-08-27 Union Carbide Cheimcals & Plastics Technology Llc. Corporation Trust Center Wood Preservative Composition
US20100062166A1 (en) * 2007-01-17 2010-03-11 Genics Inc. Preservative compositions for wood and like materials
CN1883897B (en) * 2006-06-13 2010-09-15 上海大不同木业科技有限公司 Wood protective agent
US8277911B2 (en) 2006-07-07 2012-10-02 Rengo Co., Ltd. Anticorrosion composition
US8747909B2 (en) 2003-04-09 2014-06-10 Osmose, Inc. Micronized wood preservative formulations
US9247734B2 (en) 2014-05-23 2016-02-02 Robert Sabin Potentiation of fixed coppers and other pesticides containing copper and supplementing plant nutrition
US9271502B2 (en) 2014-05-23 2016-03-01 Robert Sabin Potentiation of fixed coppers and other pesticides containing copper and supplementing plant nutrition
JP2016124849A (en) * 2015-01-08 2016-07-11 株式会社ザイエンス Antifungal composition, antifungal treatment method for woody material, and woody material
US9487453B2 (en) 2014-05-23 2016-11-08 Robert Sabin Potentiation of fixed coppers and other pesticides containing copper and supplementing plant nutrition
US9586871B2 (en) 2014-05-23 2017-03-07 Robert Sabin Potentiation of fixed coppers and other pesticides containing copper and supplementing plant nutrition
US9718739B2 (en) 2014-05-23 2017-08-01 Robert Sabin Potentiation of fixed coppers and other pesticides containing copper and supplementing plant nutrition
US10059026B2 (en) 2014-06-30 2018-08-28 Dow Global Technologies Llc Process for treating wood
US10166693B2 (en) 2014-06-30 2019-01-01 Dow Global Technologies Llc Treated porous material
US10201909B2 (en) 2014-06-30 2019-02-12 Dow Global Technologies Llc Treated wood material
US10300623B2 (en) 2014-06-30 2019-05-28 Dow Global Technologies Llc Treated porous material
US10335975B2 (en) 2014-06-30 2019-07-02 Dow Global Technologies Llc Process for treating wood

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DE3639063A1 (en) 1988-05-19
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GR3002257T3 (en) 1992-12-30
EP0270848A1 (en) 1988-06-15
ES2022863B3 (en) 1991-12-16
AU599165B2 (en) 1990-07-12
NZ222526A (en) 1989-09-27
EP0270848B1 (en) 1991-07-03
CA1305834C (en) 1992-08-04
AU8118987A (en) 1988-05-19

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